Energy expenditure and the body cell mass in Cystic Fibrosis

Shepherd, Ross, Greer, Ristan, McNaughton, Sarah, Wotton, Marita and Cleghorn, Geoffrey 2001, Energy expenditure and the body cell mass in Cystic Fibrosis, Nutrition, vol. 17, no. 1, pp. 22-25, doi: 10.1016/S0899-9007(00)00470-6.

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Title Energy expenditure and the body cell mass in Cystic Fibrosis
Author(s) Shepherd, Ross
Greer, Ristan
McNaughton, SarahORCID iD for McNaughton, Sarah
Wotton, Marita
Cleghorn, Geoffrey
Journal name Nutrition
Volume number 17
Issue number 1
Start page 22
End page 25
Publisher Nutrition
Place of publication Burbank, Calif.
Publication date 2001-01
ISSN 0899-9007
Keyword(s) cystic fibrosis
resting energy expenditure
total body potassium
body-cell mass
pulmonary function
Summary Poor nutritional status in patients with cystic fibrosis (CF) is associated with severe lung disease, and possible causative factors include inadequate intake, malabsorption, and increased energy requirements. Body cell mass (which can be quantified by measurement of total body potassium) provides an ideal standard for measurements of energy expenditure. The aim of this study was to compare resting energy expenditure (REE) in patients with CF with both predicted values and age-matched healthy children and to    determine whether REE was related to either nutritional status or pulmonary function. REE was measured by indirect calorimetry and body cell mass by scanning with total body potassium in 30 patients with CF (12 male, mean AGE = 13.07 ± 0.55 y) and 18 healthy children (six male, mean AGE = 12.56 ± 1.25 y). Nutritional status was expressed as a percentage of predicted total body potassium. Lung function was measured in the CF group by spirometry and expressed as the percentage of predicted forced expiratory volume in 1 s. Mean REE was significantly increased in the patients with CF compared with healthy children (119.3 ± 3.1% predicted versus 103.6 ± 5% predicted, P < 0.001) and, using multiple regression techniques, REE for total body potassium was significantly increased in patients with CF (P = 0.0001). There was no relation between REE and nutritional status or pulmonary disease status in the CF group. In conclusion, REE is increased in children and adolescents with CF but is not directly related to nutritional status or pulmonary disease.
Language eng
DOI 10.1016/S0899-9007(00)00470-6
Field of Research 111199 Nutrition and Dietetics not elsewhere classified
Socio Economic Objective 970111 Expanding Knowledge in the Medical and Health Sciences
HERDC Research category C1.1 Refereed article in a scholarly journal
Copyright notice ©2001, Elsevier Science Inc.
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